(Q79435491)

English

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: suggestive linkage to 10q23.32-q25.3.

scientific article published on 01 March 2007

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Europe PubMed Central

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23 December 2019

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: suggestive linkage to 10q23.32-q25.3. (English)

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Europe PubMed Central

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23 December 2019

Tommy Martinsson

4

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23 December 2019

Staffan Nilsson

6

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23 December 2019

Margareta Nordling

9

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23 December 2019

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Annika Bergman

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23 December 2019

Per Karlsson

2

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23 December 2019

Jonna Berggren

3

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23 December 2019

Karin Björck

5

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23 December 2019

Jan Wahlström

7

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23 December 2019

Arne Wallgren

8

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23 December 2019

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1 March 2007

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23 December 2019

Genes, Chromosomes and Cancer

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23 December 2019

46

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23 December 2019

3

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23 December 2019

302-309

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23 December 2019

Polygenic inheritance of breast cancer: Implications for design of association studies

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A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques

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Polymorphisms in DNA repair gene XRCC1 and increased genetic susceptibility to breast cancer

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Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p

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Allegro, a new computer program for multipoint linkage analysis

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Molecular classification of familial non-BRCA1/BRCA2 breast cancer

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Genome-wide scanning for linkage in Finnish breast cancer families

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Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus

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Pooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions

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7 January 2021

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

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High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer

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Polygenic susceptibility to breast cancer and implications for prevention

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

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Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families

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Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer

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20q11.1 amplification in giant-cell tumor of bone: Array CGH, FISH, and association with outcome.

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Mutations in SUFU predispose to medulloblastoma

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SAFB2, a new scaffold attachment factor homolog and estrogen receptor corepressor

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Identifiers

10.1002/GCC.20405

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17171685%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17171685%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

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